Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | 0.0077 | 0.3351 | 1 | |
Loa Loa (eye worm) | DOMON domain-containing protein | 0.0077 | 0.3351 | 1 |
Echinococcus multilocularis | ankyrin repeat protein | 0.0192 | 0.9765 | 0.9742 |
Leishmania major | hypothetical protein, conserved | 0.0034 | 0.092 | 0.5 |
Brugia malayi | Muscle positioning protein 4 | 0.0077 | 0.3351 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0077 | 0.3351 | 0.3431 |
Schistosoma mansoni | hypothetical protein | 0.0034 | 0.092 | 0.0942 |
Toxoplasma gondii | kringle domain-containing protein | 0.0034 | 0.092 | 0.5 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0034 | 0.092 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0077 | 0.3351 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0077 | 0.3351 | 1 |
Onchocerca volvulus | 0.0077 | 0.3351 | 1 | |
Plasmodium vivax | cysteine repeat modular protein 1, putative | 0.0034 | 0.092 | 0.5 |
Echinococcus granulosus | transient receptor potential cation channel | 0.0196 | 0.9984 | 1 |
Onchocerca volvulus | 0.0077 | 0.3351 | 1 | |
Plasmodium falciparum | cysteine repeat modular protein 1 | 0.0034 | 0.092 | 0.5 |
Brugia malayi | SEA domain containing protein | 0.0077 | 0.3351 | 1 |
Echinococcus granulosus | ankyrin repeat protein | 0.0192 | 0.9765 | 0.9759 |
Schistosoma mansoni | transient receptor potential cation channel subfamily A member | 0.0192 | 0.9765 | 1 |
Onchocerca volvulus | 0.0077 | 0.3351 | 1 | |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0025 | 0.0414 | 0.0424 |
Onchocerca volvulus | 0.0077 | 0.3351 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Efficacy (functional) | < 10 % | Agonist activity at rat TRPA1 ion channel expressed in HEK293 cells assessed as calcium influx by fluo-4-Am-based fluorimetry relative to allyl isothiocyanate | ChEMBL. | 22257892 |
Efficacy (functional) | < 10 % | Agonist activity at human TRPV1 ion channel expressed in HEK293 cells assessed as calcium influx by fluo-4-Am-based fluorimetry relative to ionomycin | ChEMBL. | 22257892 |
IC50 (functional) | > 100 uM | Antagonist activity at human TRPV1 ion channel expressed in HEK293 cells assessed as inhibition of capsaicin-induced calcium influx incubated for 5 mins prior to capsicin-induction by fluo-4-AM-based fluorimetry | ChEMBL. | 22257892 |
IC50 (functional) | > 100 uM | Antagonist activity at rat TRPA1 ion channel expressed in HEK293 cells assessed as inhibition of AITC-induced calcium influx incubated for 5 mins prior to AITC-induction by fluo-4-AM-based fluorimetry | ChEMBL. | 22257892 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
1 literature reference was collected for this gene.